The invention is generally related to the field of interconnect layers in semiconductor devices and more specifically to diffusion barriers for copper interconnect layers.
As the density of semiconductor devices increases, the demands on interconnect layers for connecting the semiconductor devices to each other also increases. Therefore, there is a desire to switch from the traditional aluminum metal interconnects to copper interconnects. Unfortunately, suitable copper etches for a semiconductor fabrication environment are not readily available. To overcome the copper etch problem, damascene processes have been developed.
In a damascene process, the IMD is formed first. The IMD is then patterned and etched. The barrier layer 14 and a copper seed layer are then deposited over the structure. The barrier layer 14 is typically tantalum, tantalum nitride or some other binary transition metal nitride. The copper layer is deposited by electroplating over the seed layer. The copper is then chemically-mechanically polished (CMP′d) to remove the copper from over the IMD 16, leaving copper interconnect lines 18 as shown in
Barrier layer 14 is required because copper has high diffusivity. Copper interconnects totally rely on the encapsulating barrier materials to prevent copper from diffusing through to cause leakage and transistor poisoning. The basic requirements for the barrier materials are 1) good barrier efficiency, 2) good copper wettability, and 3) strong copper to barrier bonding. The most commonly used barrier materials to date are TiN, Ta, and TaN. TiN and Ta do not meet the first criterion very well although Ta is a little better than TiN. If TiN or Ta is used as the barrier material in copper interconnects, a relatively thick layer of barrier material is required in vias and trenches. This becomes less and less viable as device geometries shrink. TaN has near amorphous structure and therefore, it has a better barrier efficiency. However, TaN, does not meet the last two criteria well. Copper does not like to wet to TaN surfaces and tends to detach from TaN due to the weak bonding strength. This causes voids in the copper during the via fill and negatives impacts the electromigration performance. Metal-silicon-nitrides have better wetting properties. Unfortunately, current methods of forming these metal-silicon-nitrides are difficult to perform and result in a film having high resistivity.
The invention is a copper interconnect having a transition metal-silicon-nitride barrier. A transition metal-nitride is co-deposited with Si using a reactive sputter deposition in a Si-containing ambient. The copper is then deposited over the transition metal-silicon-nitride barrier layer.
An advantage of the invention is providing a diffusion barrier having improved adhesion with copper, low resistance, and that can be fabricated using a method that offers higher throughput and is easy to implement.
This and other advantages will be apparent to those of ordinary skill in the art having reference to the specification in conjunction with the drawings.
In the drawings:
The invention will now be described in conjunction with a copper interconnect layer. Those of ordinary skill in the art will realize that the benefits of the invention may be applied to diffusion barriers in general where improved wetting property is desired without a significant increase in resistance.
A transition metal-silicon-nitride diffusion barrier 106, according to the invention, is shown in
Suitable materials for ILD 102 and IMD 104 are known in the art. ILD 102 and IMD 104 may comprise the same or differing materials. For example, ILD 102 and IMD 104 may comprise a PETEOS (Plasma Enhanced TetraEthyOxySilane) oxide or a low-k material such as xerogel, FSG (fluorine-doped silicate glass), HSQ (Hydrogen SilesQuixane) organic low-k materials, or a combination thereof.
Diffusion barrier 106 is located within in ILD 102 and IMD 104. Diffusion barrier 106 comprises a transition metal-silicon-nitride. For example, diffusion barrier 106 may comprise TaSiN or WSiN. Copper 110 is located over barrier 106. The transition metal-silicon-nitride diffusion barrier 106 has low resistance and excellent wettability to dielectrics such as FSG. While transition metal-nitrides have poor wettability to copper. The metal-silicon-nitrides, on the other hand, have good wettability to copper. While some metal-silicon-nitrides have higher resistivity, metal-silicon nitrides formed according to the invention have comparable resistivity to metal-nitrides as long as the N:Si ratio is kept low (i.e., N:Si<0.6). High N content is believed to cause the formation of Si3N4. Si3N4 has higher resistivity and increases the total resistivity of the metal-silicon-nitride film.
As shown in Table I, TaSiN is amorphous, whereas TaN is only near amorphous. Amorphous layers tend to be good barriers for copper because they do not have grain boundaries for the copper to diffuse through.
The sidewall agglomeration for copper is also very good for TaSiN. On TaN, copper forms large islands and thus, voids in the copper which are bad for electromigration. On Ta, copper forms small islands, which are better, but not as good as the near continuous layer of TaSiN.
A method for forming diffusion barrier 106, according to the invention, will now be discussed with reference to
Referring to
Next, a diffusion barrier 106 is formed on the surface of IMD 104 and on the surface of trench 120, as shown in
Transition metal-silicon nitride is formed by co-depositing Si and the transition metal-nitride. The transition metal-nitride is deposited by reactive sputtering. A Si-containing ambient may be used to co-deposit the Si. As an example, silicon-containing gases such as SiH4, Si2H6, or Si(NR3)4, where R is an organic ligand may be used with a Ta target and a nitrogen-containing gas. The amount of Si incorporated in the barrier film 106 can be controlled by the gas flow of the silicon containing gas. This method gives total flexibility of the Si concentration in the barrier film 106. If desired, a linear or non-linear gradient of Si concentration can be generated inside the barrier film 106 by varying the cas flow during deposition. Alternatively, a TaSi target may be used.
The N:Si ratio is kept low. The low N:Si ratio results in lower sheet resistance. A sheet resistance monitor may be employed to ensure low resistance.
Barrier film 106 can be deposited using low temperatures (i.e., <˜250° C.). Low temperatures are more compatible with multilayer interconnect processing technology.
Physical Vapor Deposition (PVD) systems are used for reactive sputtering. Modifications to the typical pump system of a PVD system are needed. The typical pump system uses a cryo pump. The cryo pump is not appropriate for the invention. A turbo pump should be added to accomplish the invention.
The transition metal-silicon-nitride film is totally amorphous and provides good wettability to the subsequently formed copper. Lower resistivity can be obtained by keeping the N:Si ratio low. For example, resistivities less than 250 μΩ/cm have been achieved. The above method for forming the transition metal silicon nitride is an in-situ process that allows higher throughput that ex-situ processes. No vacuum break is needed which eliminates the formation of a barrier oxide.
Referring to
The copper layer 110 and barrier layer 106 are then removed back, for example by CMP (chemical-mechanical polish) to substantially planar with IMD 104, as shown in
The transition metal-silicon-nitride diffusion barrier 106 may be applied to the first or any subsequent copper interconnect layer. Furthermore, it may be applied to one, some, or all of the copper interconnect layers.
While this invention has been described with reference to illustrative embodiments, this description is not intended to be construed in a limiting sense. Various modifications and combinations of the illustrative embodiments, as well as other embodiments of the invention, will be apparent to persons skilled in the art upon reference to the description. It is therefore intended that the appended claims encompass any such modifications or embodiments.
This application claims priority under 35 USC §119(e)(1) of provisional application No. 60/221,248 filed Jul. 27, 2000. The following co-pending application is related and hereby incorporated: Ser. No. 60/150,996 Filed Aug. 27, 1999 Inventors Lu et al.
Number | Name | Date | Kind |
---|---|---|---|
4201999 | Howard et al. | May 1980 | A |
4829363 | Thomas et al. | May 1989 | A |
4873205 | Critchlow et al. | Oct 1989 | A |
5686355 | Sumi et al. | Nov 1997 | A |
5796166 | Agnello et al. | Aug 1998 | A |
5926740 | Forbes et al. | Jul 1999 | A |
5980265 | Tischler | Nov 1999 | A |
6093966 | Venkatraman et al. | Jul 2000 | A |
6153519 | Jain et al. | Nov 2000 | A |
6181012 | Edelstein et al. | Jan 2001 | B1 |
6246082 | Mitarai et al. | Jun 2001 | B1 |
6376371 | Jain et al. | Apr 2002 | B1 |
6399496 | Edelstein et al. | Jun 2002 | B1 |
6500742 | Chern et al. | Dec 2002 | B1 |
6661057 | Dawson et al. | Dec 2003 | B1 |
6797608 | Lin | Sep 2004 | B1 |
Number | Date | Country | |
---|---|---|---|
20020001944 A1 | Jan 2002 | US |
Number | Date | Country | |
---|---|---|---|
60221248 | Jul 2000 | US |